The role of dctP gene in regulating colonization, adhesion and pathogenicity of Vibrio alginolyticus strain HY9901.
Vibrio alginolyticus
adhesion
colonization
dctP gene
virulence
Journal
Journal of fish diseases
ISSN: 1365-2761
Titre abrégé: J Fish Dis
Pays: England
ID NLM: 9881188
Informations de publication
Date de publication:
Mar 2022
Mar 2022
Historique:
revised:
29
11
2021
received:
22
10
2021
accepted:
03
12
2021
pubmed:
22
12
2021
medline:
11
2
2022
entrez:
21
12
2021
Statut:
ppublish
Résumé
Vibriosis caused by Vibrio alginolyticus has severely affected the development of mariculture industry in recent decades. DctP, a tripartite ATP-independent periplasmic transporter solute-binding subunit, is thought to be one of the virulence factors in Vibrio. In this study, the results displayed no difference in morphological characteristics and growth between ΔdctP (dctP mutant strain) and WT (wild-type strain). Nevertheless, the ability of swarming motility, biofilm formation, ECPase formation, cell adhesion and colonized ability of ΔdctP significantly decreased compared to those of WT. The LD
Substances chimiques
Bacterial Proteins
0
Virulence Factors
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
421-434Subventions
Organisme : National Natural Science Foundation of China
ID : U20A2065
Organisme : Fund of Southern Marine Science and Engineering Guangdong Laboratory
ID : ZJW-2019-06
Organisme : Guangdong Natural Science Foundation
ID : 2021A1515010532
Informations de copyright
© 2021 John Wiley & Sons Ltd.
Références
Almagro-Moreno, S., Pruss, K., & Taylor, R. K. (2015). Intestinal colonization dynamics of Vibrio cholerae. PLoS Path, 11, e1004787. https://doi.org/10.1371/journal.ppat.1004787
Bai, F., Pang, L., Qi, Z., Chen, J., Austin, B., & Zhang, X. H. (2008). Distribution of five vibrio virulence-related genes among Vibrio harveyi isolates. The Journal of Genenal Applied Microbiology, 54, 71-78. https://doi.org/10.2323/jgam.54.71
Baker, M. D., Wolanin, P. M., & Stock, J. B. (2006). Signal transduction in bacterial chemotaxis. Bioessays: News and Reviews in Molecular, Cellular and Developmental Biology. 28(1), 9-22. https://doi.org/10.1002/bies.20343
Bunpa, S., Chaichana, N., Teng, J. L. L., Lee, H. H., Woo, P. C. Y., Sermwittayawong, D., Nongyao, S., & Natthawan, S. (2020). Outer membrane protein A (OmpA) is a potential virulence factor of Vibrio alginolyticus strains isolated from diseased fish. Journal of Fish Diseases, 43, 275-284. https://doi.org/10.1111/jfd.13120
Cai, J., Zou, Z., Wei, S., Zheng, Q., Xu, Y., Lu, Y., Wu, Z., Qin, Q., & Jian, J. (2019). Identification of Beclin-1 from orange-spotted grouper (Epinephelus coioides) involved in viral infection. Fish & Shellfish Immunology, 94, 336-345. https://doi.org/10.1016/j.fsi.2019.09.029
Cai, S., Cheng, H., Pang, H., Jian, J., & Wu, Z. (2018). AcfA is an essential regulator for pathogenesis of fish pathogen Vibrio alginolyticus. Veterinary Microbiology, 213, 35-41. https://doi.org/10.1016/j.vetmic.2017.11.016
Cai, S., Wu, Z., Jian, J., & Lu, Y. (2007). Cloning and expression of gene encoding the thermostable direct hemolysin from Vibrio alginolyticus strain HY9901, the causative agent of vibriosis of crimson snapper (Lutjanus erythopterus). Journal of Applied Microbiology, 103, 289-296. https://doi.org/10.1111/j.1365-2672.2006.03250.x
Chen, Y., Cai, S., & Jian, J. (2019). Protection against Vibrio alginolyticus in pearl gentian grouper (♀Epinephelus fuscoguttatus × ♂Epinephelus lanceolatu) immunized with an acfA-deletion live attenuated vaccine. Fish & Shellfish Immunology, 86, 875-881. https://doi.org/10.1016/j.fsi.2018.12.030
Echazarreta, M. A., & Klose, K. E. (2019). Vibrio flagellar synthesis. Frontiers in Cellular and Infection Microbiology, 9, 131. https://doi.org/10.3389/fcimb.2019.00131
Fu, S., Ni, P., Yang, Q., Hu, H., Wang, Q., Ye, S., & Liu, Y. (2020). Delineating the key virulence factors and intraspecies divergence of Vibrio harveyi via whole-genome sequencing. Canadian Journal of Microbiology, 67, 231-248. https://doi.org/10.1139/cjm-2020-0079
Fukuoka, H., Wada, T., Kojima, S., Ishijima, A., & Homma, M. (2009). Sodium-dependent dynamic assembly of membrane complexes in sodium-driven flagellar motors. Molecular Microbiology, 71, 825-835. https://doi.org/10.1111/j.1365-2958.2008.06569.x
Haiko, J., & Westerlund-Wikstrom, B. (2013). The role of the bacterial flagellum in adhesion and virulence. Biology (Basel), 2, 1242-1267. https://doi.org/10.3390/biology2041242
Huang, X., Huang, Y., Sun, J., Han, X., & Qin, Q. (2009). Characterization of two grouper Epinephelus akaara cell lines: Application to studies of Singapore grouper iridovirus (SGIV) propagation and virus-host interaction. Aquaculture, 292, 172-179. https://doi.org/10.1016/j.aquaculture.2009.04.019
Hughes, K. J., Everiss, K. D., Kovach, M. E., & Peterson, K. M. (1995). Isolation and characterization of the Vibrio cholerae acfA gene, required for efficient intestinal colonization. Gene, 156, 59-61. https://doi.org/10.1016/0378-1119(95)00054-a
Hung, D. T., Zhu, J., Sturtevant, D., & Mekalanos, J. J. (2006). Bile acids stimulate biofilm formation in Vibrio cholerae. Molecular Microbiology, 59, 193-201. https://doi.org/10.1111/j.1365-2958.2005.04846.x
Ji, Q., Wang, S., Ma, J., & Liu, Q. (2020). A review: Progress in the development of fish Vibrio spp. vaccines. Immunology Letters, 226, 46-54. https://doi.org/10.1016/j.imlet.2020.07.002
Kim, B. O., Chung, I. Y., & Cho, Y. H. (2019). Differential expression of the major catalase, KatA in the two wild type Pseudomonas aeruginosa strains, PAO1 and PA14. Journal of Microbiology, 57, 704-710. https://doi.org/10.1007/s12275-019-9225-1
Koike, M., Terashima, H., Kojima, S., & Homma, M. (2010). Isolation of basal bodies with C-ring components from the Na+ -driven flagellar motor of Vibrio alginolyticus. Journal of Bacteriology, 192, 375-378. https://doi.org/10.1128/JB.01121-09
Kojima, S., Nonoyama, N., Takekawa, N., Fukuoka, H., & Homma, M. (2011). Mutations targeting the C-terminal domain of FliG can disrupt motor assembly in the Na+ -driven flagella of Vibrio alginolyticus. Journal of Molecular Biology, 414, 62-74. https://doi.org/10.1016/j.jmb.2011.09.019
Kojima, S., Shinohara, A., Terashima, H., Yakushi, T., Sakuma, M., Homma, M., Keiichi, N., & Katsumi, I. (2008). Insights into the stator assembly of the Vibrio flagellar motor from the crystal structure of MotY. Proceedings of the National Academy of Sciences of the United States of America, 105, 7696-7701. https://doi.org/10.1073/pnas.0800308105
Lawley, T. D., & Walker, A. W. (2013). Intestinal colonization resistance. Immunology, 138, 1-11. https://doi.org/10.1111/j.1365-2567.2012.03616.x
Lee, E. M., Ahn, S. H., Park, J. H., Lee, J. H., Ahn, S. C., & Kong, I. S. (2004). Identification of oligopeptide permease (opp) gene cluster in Vibrio fluvialis and characterization of biofilm production by oppA knockout mutation. FEMS Microbiology Letters, 240, 21-30. https://doi.org/10.1016/j.femsle.2004.09.007
Li, L., Meng, H., Gu, D., Li, Y., & Jia, M. (2019). Molecular mechanisms of Vibrio parahaemolyticus pathogenesis. Microbiological Research, 222, 43-51. https://doi.org/10.1016/j.micres.2019.03.003
Li, L., Su, Y. B., Peng, B., Peng, X. X., & Li, H. (2020). Metabolic mechanism of colistin resistance and its reverting in Vibrio alginolyticus. Environmental Microbiology, 22, 4295-4313. https://doi.org/10.1111/1462-2920.15021
Liu, S. R., Peng, X. X., & Li, H. (2019). Metabolic mechanism of ceftazidime resistance in Vibrio alginolyticus. Infection and Drug Resistence, 12, 417-429. https://doi.org/10.2147/IDR.S179639
Low, C. F., Shamsudin, M. N., Chee, H. Y., Aliyu-Paiko, M., & Idrus, E. S. (2014). Putative apolipoprotein A-I, natural killer cell enhancement factor and lysozyme g are involved in the early immune response of brown-marbled grouper, Epinephelus fuscoguttatus, Forskal, to Vibrio alginolyticus. Journal of Fish Disease, 37, 693-701. https://doi.org/10.1111/jfd.12153
Luo, G., Huang, L., Su, Y., Qin, Y., Xu, X., Zhao, L., & Yan, Q. (2016). flrA, flrB and flrC regulate adhesion by controlling the expression of critical virulence genes in Vibrio alginolyticus. Emerging Microbes & Infections, 5, e85. https://doi.org/10.1038/emi.2016.82
Luo, G., Xu, X., Zhao, L., Qin, Y., Huang, L., Su, Y., & Yan, Q. (2019). clpV is a key virulence gene during in vivo Pseudomonas plecoglossicida infection. Journal of Fish Disease, 42, 991-1000. https://doi.org/10.1111/jfd.13001
Martin, A. H., Rosemarie, C. R., & Robert, V. T. (1977). Trimmed Spearman-Karber method for estimating median lethal concentrations in toxicity bioassays. Environmental Science & Technology, 11, 714-717. https://doi.org/10.1021/es60130a004
Mulligan, C., Fischer, M., & Thomas, G. H. (2011). Tripartite ATP-independent periplasmic (TRAP) transporters in bacteria and archaea. FEMS Microbiology Reviews, 35, 68-86. https://doi.org/10.1111/j.1574-6976.2010.00236.x
O'Boyle, N., Houeix, B., Kilcoyne, M., Joshi, L., & Boyd, A. (2013). The MSHA pilus of Vibrio parahaemolyticus has lectin functionality and enables TTSS-mediated pathogenicity. International Journal of Medical Microbiology: IJMM, 303, 563-573. https://doi.org/10.1016/j.ijmm.2013.07.010
Ogawa, R., Abe-Yoshizumi, R., Kishi, T., Homma, M., & Kojima, S. (2015). Interaction of the C-terminal tail of FliF with FliG from the Na+ -driven flagellar motor of Vibrio alginolyticus. Journal of Bacteriology, 197, 63-72. https://doi.org/10.1128/JB.02271-14
Okabe, M., Yakushi, T., & Homma, M. (2005). Interactions of MotX with MotY and with the PomA/PomB sodium ion channel complex of the Vibrio alginolyticus polar flagellum. The Journal of Biological Chemistry, 280, 25659-25664. https://doi.org/10.1074/jbc.M500263200
Osei-Adjei, G., Huang, X., & Zhang, Y. (2018). The extracellular proteases produced by Vibrio parahaemolyticus. World Journal of Microbiology & Biotechnology, 34, 68. https://doi.org/10.1007/s11274-018-2453-4
O'Toole, G., Kaplan, H. B., & Kolter, R. (2000). Biofilm formation as microbial development. Annual Review of Microbiology, 54, 49-79. https://doi.org/10.1146/annurev.micro.54.1.49
Pang, H., Qiu, M., Zhao, J., Hoare, R., Monaghan, S. J., Song, D., Chang, Y., & Jian, J. (2018). Construction of a Vibrio alginolyticus hopPmaJ (hop) mutant and evaluation of its potential as a live attenuated vaccine in orange-spotted grouper (Epinephelus coioides). Fish & Shellfish Immunology, 76, 93-100. https://doi.org/10.1016/j.fsi.2018.02.012
Peterson, K. M., & Mekalanos, J. J. (1988). Characterization of the Vibrio cholerae ToxR regulon: Identification of novel genes involved in intestinal colonization. Infection and Immunity, 56, 2822-2829. https://doi.org/10.1128/iai.56.11.2822-2829.1988
Pratt, J. T., Ismail, A. M., & Camilli, A. (2010). PhoB regulates both environmental and virulence gene expression in Vibrio cholerae. Molecular Microbiology, 77, 1595-1605. https://doi.org/10.1111/j.1365-2958.2010.07310.x
Provenzano, D., & Klose, K. E. (2000). Altered expression of the ToxR-regulated porins OmpU and OmpT diminishes Vibrio cholerae bile resistance, virulence factor expression, and intestinal colonization. Proceedings of the National Academy of Sciences of the United States of America, 97, 10220-10224. https://doi.org/10.1073/pnas.170219997
Rhie, M. N., Park, B., Ko, H. J., Choi, I. G., & Kim, O. B. (2018). Transcriptome analysis and anaerobic C4 -dicarboxylate transport in Actinobacillus succinogenes. MicrobiologyOpen, 7, e00565. https://doi.org/10.1002/mbo3.565
Sharma, S. K., Moe, T. S., Srivastava, R., Chandra, D., & Srivastava, B. S. (2011). Functional characterization of VC1929 of Vibrio cholerae El Tor: Role in mannose-sensitive haemagglutination, virulence and utilization of sialic acid. Microbiology (Reading), 157, 3180-3186. https://doi.org/10.1099/mic.0.050245-0
Song, H., Kang, Y., Qian, A., Shan, X., Li, Y., Zhang, L., Zhang, H., & Sun, W. (2020). Inactivation of the T6SS inner membrane protein DotU results in severe attenuation and decreased pathogenicity of Aeromonas veronii TH0426. BMC Microbiology, 20, 76. https://doi.org/10.1186/s12866-020-01743-5
Terashima, H., Fukuoka, H., Yakushi, T., Kojima, S., & Homma, M. (2006). The Vibrio motor proteins, MotX and MotY, are associated with the basal body of Na+ -driven flagella and required for stator formation. Molecular Microbiology, 62, 1170-1180. https://doi.org/10.1111/j.1365-2958.2006.05435.x
Ushijima, B., Videau, P., Poscablo, D., Stengel, J. W., Beurmann, S., Burger, A. H., Greta, S. A., & Sean, M. C. (2016). Mutation of the toxR or mshA genes from Vibrio coralliilyticus strain OCN014 reduces infection of the coral Acropora cytherea. Environmental Microbiology, 18, 4055-4067. https://doi.org/10.1111/1462-2920.13428
Valentini, M., Storelli, N., & Lapouge, K. (2011). Identification of C4 -dicarboxylate transport systems in Pseudomonas aeruginosa PAO1. Journal of Bacteriology, 193, 4307-4316. https://doi.org/10.1128/JB.05074-11
Walmsley, A. R., Shaw, J. G., & Kelly, D. J. (1992). Perturbation of the equilibrium between open and closed conformations of the periplasmic C4 -dicarboxylate binding protein from Rhodobacter capsulatus. Biochemistry, 31, 11175-11181. https://doi.org/10.1021/bi00160a031
Wang, L., Huang, L., Su, Y., Qin, Y., Kong, W., Ma, Y., Xu, X., Lin, M., Zheng, J., & Yan, Q. (2015). Involvement of the flagellar assembly pathway in Vibrio alginolyticus adhesion under environmental stresses. Frontiers in Cellular and Infection Microbiology, 5, 59. https://doi.org/10.3389/fcimb.2015.00059
Whitaker, W. B., Parent, M. A., Boyd, A., Richards, G. P., & Boyd, E. F. (2012). The Vibrio parahaemolyticus ToxRS regulator is required for stress tolerance and colonization in a novel orogastric streptomycin-induced adult murine model. Infection and Immunity, 80, 1834-1845. https://doi.org/10.1128/IAI.06284-11
Xie, L., Altindal, T., Chattopadhyay, S., & Wu, X. L. (2011). From the cover: Bacterial flagellum as a propeller and as a rudder for efficient chemotaxis. Proceedings of the National Academy of Sciences of the United States of America, 108, 2246-2251. https://doi.org/10.1073/pnas.1011953108
Xiong, X. P., Wang, C., Ye, M. Z., Yang, T. C., Peng, X. X., & Li, H. (2010). Differentially expressed outer membrane proteins of Vibrio alginolyticus in response to six types of antibiotics. Marine Biotechnology (NY), 12, 686-695. https://doi.org/10.1007/s10126-009-9256-4
Xu, X., Li, H., Qi, X., Chen, Y., Qin, Y., Zheng, J., & Jiang, X. (2020). cheA, cheB, cheR, cheV, and cheY are involved in regulating the adhesion of Vibrio harveyi. Frontiers in Cellular and Infection Microbiology, 10, 591751. https://doi.org/10.3389/fcimb.2020.591751
Zhang, S., Wang, J., Jiang, M., Xu, D., Peng, B., Peng, X. X., & Li, H. (2019). Reduced redox-dependent mechanism and glucose-mediated reversal in gentamicin-resistant Vibrio alginolyticus. Environmental Microbiology, 21, 4724-4739. https://doi.org/10.1111/1462-2920.14811